A clinical study and future prospects for bioactive compounds and semi-synthetic molecules in the therapies for Huntington's disease
Author:
Publisher
Springer Science and Business Media LLC
Subject
Neuroscience (miscellaneous),Cellular and Molecular Neuroscience,Neurology
Link
https://link.springer.com/content/pdf/10.1007/s12035-023-03604-4.pdf
Reference339 articles.
1. Krobitsch S, Kazantsev AG (2011) Huntington’s disease: from molecular basis to therapeutic advances. Int J Biochem Cell Biol 43:20–24. https://doi.org/10.1016/J.BIOCEL.2010.10.014
2. Kumar P, Kalonia H, Kumar A (2010) Huntington’s disease: pathogenesis to animal models. Pharmacol Rep 62:1–14. https://doi.org/10.1016/S1734-1140(10)70238-3
3. Ross CA, Aylward EH, Wild EJ, Langbehn DR, Long JD, Warner JH, Scahill RI, Leavitt BR et al (2014) Huntington disease: natural history, biomarkers and prospects for therapeutics. Nat Rev Neurol 10(4):204–16. https://doi.org/10.1038/nrneurol.2014.24
4. Gil JM, Rego AC (2008) Mechanisms of neurodegeneration in Huntington’s disease. Eur J Neurosci 27:2803–2820. https://doi.org/10.1111/J.1460-9568.2008.06310.X
5. Bashir H (2019) Emerging therapies in Huntington’s disease. Expert Rev Neurother 19:983–995. https://doi.org/10.1080/14737175.2019.1631161
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